FDA Inspection 602253 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 1000476619

The FDA completed an inspection of Sanofi Winthrop Industrie on July 17, 2009 in Sisteron. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 17, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sisteron (France)